2000
[DOCID: f:s708is.txt]
107th CONGRESS
1st Session
S. 708
To provide the citizens of the United States and Congress with a report
on coordinated actions by Federal agencies to prevent the introduction
of foot and mouth disease and bovine spongiform encephalopathy into the
United States and other information to assess the economic and public
health impacts associated with the potential threats presented by those
diseases.
_______________________________________________________________________
IN THE SENATE OF THE UNITED STATES
April 5, 2001
Mr. Hatch (for himself, Mr. Harkin, Mr. Campbell, Mr. Durbin, Mr.
Daschle, Mr. Roberts, Mr. Dayton, Mr. Conrad, Mr. Dorgan, Mr. Johnson,
Mr. Feingold, Mr. Kohl, Mr. Nelson of Nebraska, Mr. Grassley, Mr.
Lugar, Mr. Bond, Mr. Brownback, Mrs. Feinstein, Mr. Akaka, Mr.
Bingaman, Mr. Baucus, Mr. Burns, Mr. Craig, Mr. Enzi, Mr. Thomas, Mrs.
Lincoln, Mr. Edwards, Mr. Hollings, Mr. Helms, Mrs. Clinton, Mr. Crapo,
Ms. Mikulski, Mr. Leahy, Mr. Fitzgerald, Mr. Wyden, Mr. Rockefeller,
Mr. Allard, and Ms. Stabenow) introduced the following bill; which was
read twice and referred to the Committee on Agriculture, Nutrition, and
Forestry
_______________________________________________________________________
A BILL
To provide the citizens of the United States and Congress with a report
on coordinated actions by Federal agencies to prevent the introduction
of foot and mouth disease and bovine spongiform encephalopathy into the
United States and other information to assess the economic and public
health impacts associated with the potential threats presented by those
diseases.
Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the ``Animal Disease Risk Assessment,
Prevention, and Control Act of 2001''.
SEC. 2. FINDINGS AND PURPOSE.
(a) Findings.--Congress finds that--
(1) it is in the interest of the United States to maintain
healthy livestock herds;
(2) managing the risks of foot and mouth disease, bovine
spongiform encephalopathy, and related diseases in the United
States may require billions of dollars for remedial activities
by consumers, producers, and distributors of meat and blood
products;
(3) the potential introduction of those diseases into the
United States would cause devastating financial losses to--
(A) the agriculture industry and other economic
sectors; and
(B) United States trade in the affected animals and
animal products;
(4) foot and mouth disease is a severe and highly
contagious viral infection affecting cattle, deer, goats,
sheep, swine, and other animals;
(5) the most effective means of eradicating foot and mouth
disease is by the slaughter of affected animals;
(6) while foot and mouth disease was eradicated in the
United States in 1929, the virus could be reintroduced by--
(A) a single infected animal, an animal product, or
a person carrying the virus;
(B) an act of terrorism; or
(C) other means;
(7) once introduced, foot and mouth disease can spread
quickly through--
(A) exposure to aerosols from infected animals;
(B) direct contact with infected animals; and
(C) contact with contaminated feed, equipment, or
humans harboring the virus or carrying the virus on
their clothing;
(8) foot and mouth disease is endemic to more than \2/3\ of
the world and is considered to be widespread in parts of
Africa, Asia, Europe, and South America;
(9) foot and mouth disease occurs in over 7 different
serotypes and 60 subtypes;
(10) as foot and mouth disease outbreaks have occurred, the
United States has banned the importation of live ruminants and
swine and many animal products from countries affected by foot
and mouth disease;
(11) recently, the United States has implemented bans in
response to outbreaks in Argentina, the European Union, and
Taiwan;
(12) although United States exclusion programs have been
successful at keeping foot and mouth disease out of the United
States since 1929, recent outbreaks in Argentina, the European
Union, and Taiwan are placing an unprecedented strain on our
animal health system;
(13) bovine spongiform encephalopathy is a transmissible,
neuro-degenerative disease found in cattle;
(14) in cattle with bovine spongiform encephalopathy, the
active agent is found primarily in the brain and spinal cord
and has not been found in commonly consumed beef products;
(15) bovine spongiform encephalopathy is thought to have an
incubation period of several years but is ultimately fatal to
cattle within weeks of onset of the active disease;
(16) bovine spongiform encephalopathy was first widely
found in 1986 in cattle in the United Kingdom;
(17) bovine spongiform encephalopathy-carrying cattle have
been found in cattle in Belgium, Denmark, France, Germany,
Ireland, Italy, Liechtenstein, Luxembourg, the Netherlands,
Portugal, Spain, and Switzerland;
(18) cattle infected with bovine spongiform encephalopathy
originating from the United Kingdom have been found and
intercepted in Canada;
(19) since 1989, the Secretary of Agriculture has
prohibited the importation of live grazing animals from
countries where bovine spongiform encephalopathy has been found
in cattle;
(20) other products derived from grazing animals, such as
blood meal, bonemeal, fat, fetal bovine serum, glands, meat-
and-bone meal, and offal, are prohibited from entry, except
under special conditions or under permits issued by the
Secretary of Agriculture for scientific or research purposes;
(21) on December 12, 1997, the Secretary of Agriculture
extended those restrictions to include all countries in Europe
because of concerns about widespread risk factors and
inadequate surveillance for bovine spongiform encephalopathy;
(22) on December 7, 2000, the Secretary of Agriculture
prohibited all imports of rendered animal protein products from
Europe;
(23) Creutzfeldt-Jacob disease is a human spongiform
encephalopathy;
(24) on March 20, 1996, the Spongiform Encephalopathy
Advisory Committee of the United Kingdom announced the
identification of 10 cases of a new variant of Creutzfeldt-
Jacob disease;
(25) all 10 patients developed onsets of the disease in
1994 or 1995;
(26) scientific experts (including scientists at the
Department of Agriculture, the Department of Health and Human
Services, and the World Health Organization) are studying the
possible link (including potential routes of transmission)
between bovine spongiform encephalopathy and variant
Creutzfeldt-Jacob disease;
(27) from October 1996 to December 2000, 87 cases of
variant Creutzfeldt-Jacob disease have been reported in the
United Kingdom, 3 cases in France, and 1 case in Ireland; and
(28) to reduce the risk of human spongiform
encephalopathies in the United States, the Commissioner of Food
a
2000
nd Drugs has--
(A) banned individuals who lived in Great Britain
for at least 180 days since 1980 from donating blood in
the United States; and
(B) established regulations that prohibit the
feeding of most animal-derived proteins to grazing
animals.
(b) Purpose.--The purpose of this Act is to provide the people of
the United States and Congress with information concerning--
(1) actions by Federal agencies to prevent foot and mouth
disease, bovine spongiform encephalopathy, and related
diseases;
(2) the sufficiency of legislative authority to prevent or
control foot and mouth disease, bovine spongiform
encephalopathy, and related diseases in the United States;
(3) the economic impacts associated with the potential
introduction of foot and mouth disease, bovine spongiform
encephalopathy, and related diseases into the United States;
and
(4) the risks to public health from possible links between
bovine spongiform encephalopathy and other spongiform
encephalopathies to human illnesses.
SEC. 3. REPORT TO CONGRESS.
(a) Preliminary Report.--
(1) In general.--Not later than 30 days after the date of
enactment of this Act, the Secretary of Agriculture shall
submit to the Committees and Subcommittees described in
paragraph (2) a preliminary report concerning--
(A) coordinated interagency activities to assess,
prevent, and control the spread of foot and mouth
disease and bovine spongiform encephalopathy in the
United States;
(B) sources of information from the Federal
Government available to the public on foot and mouth
disease and bovine spongiform encephalopathy; and
(C) any immediate needs for additional legislative
authority, appropriations, or product bans to prevent
the introduction of foot and mouth disease or bovine
spongiform encephalopathy into the United States.
(2) Submission of report to congress.--The Secretary shall
submit the preliminary report to--
(A) the Committee on Agriculture of the House of
Representatives;
(B) the Committee on Agriculture, Nutrition, and
Forestry of the Senate;
(C) the Subcommittee on Agriculture, Rural
Development, and Related Agencies of the Committee on
Appropriations of the Senate; and
(D) the Subcommittee on Agriculture, Rural
Development, Food and Drug Administration, and Related
Agencies of the Committee on Appropriations of the
House of Representatives.
(b) Final Report.--
(1) In general.--Not later than 180 days after the date of
enactment of this Act, the Secretary of Agriculture shall
submit to the Committees and Subcommittees described in
subsection (a)(2) a final report that--
(A) discusses the economic impacts associated with
the potential introduction of foot and mouth disease,
bovine spongiform encephalopathy, and related diseases
into the United States;
(B) discusses the potential risks to public and
animal health from foot and mouth disease, bovine
spongiform encephalopathy, and related diseases; and
(C) provides recommendations to protect the health
of animal herds and citizens of the United States from
those risks including, if necessary, recommendations
for additional legislation, appropriations, or product
bans.
(2) Contents.--The report shall contain--
(A) an assessment of the risks to the public
presented by the potential presence of foot and mouth
disease, bovine spongiform encephalopathy, and related
diseases in domestic and imported livestock, livestock
and animal products, wildlife, and blood products;
(B) recommendations to reduce and manage the risks
of foot and mouth disease, bovine spongiform
encephalopathy, and related diseases;
(C) any plans of the Secretary to identify,
prevent, and control foot and mouth disease, bovine
spongiform encephalopathy, and related diseases in
domestic and imported livestock, livestock products,
wildlife, and blood products;
(D) a description of the incidence and prevalence
of foot and mouth disease, bovine spongiform
encephalopathy, variant Creutzfeldt-Jacob disease, and related diseases
in other countries;
(E) a description and an analysis of the
effectiveness of the measures taken to assess, prevent,
and control the risks of foot and mouth disease, bovine
spongiform encephalopathy, variant Creutzfeldt-Jacob
disease, and related diseases in other countries;
(F) a description and an analysis of the
effectiveness of the measures that the public, private,
and nonprofit sectors have taken to assess, prevent,
and control the risk of foot and mouth disease, bovine
spongiform encephalopathy, and related diseases in the
United States, including controls of ports of entry and
other conveyances;
(G) a description of the measures taken to prevent
and control the risk of bovine spongiform
encephalopathy and variant Creutzfeldt-Jacob disease
transmission through blood collection and transfusion;
(H) a description of any measures (including any
planning or managerial initiatives such as interagency,
intergovernmental, international, and public-private
sector partnerships) that any Federal agency plans to
initiate or continue to assess, prevent, and control
the spread of foot and mouth disease, bovine spongiform
encephalopathy, variant Creutzfeldt-Jacob disease, and
related diseases in the United States and other
countries;
(I) plans by Federal agencies (including the
Centers for Disease Control and Prevention)--
(i) to monitor the incidence and prevalence
of the transmission of foot and mouth disease,
bovine spongiform encephalopathy, variant
Creutzfeldt-Jacob disease, and related diseases
in the United States; and
(ii) to assess the effectiveness of efforts
to prevent and control the spread of foot and
mouth disease, bovine spongiform
encephalopathy, variant Creutzfeldt-Jacob
disease, and related diseases in the United
States;
(J) plans by Federal agencies (including the
Agricultural Research Service, the Cooperative State
Research, Education, and Extension Service, and the
National Institutes of Health) to carry out, in
partnership with the private sector--
(i) research programs into the causes and
mechanism of transmission of foot and mouth
a3a
disease and bovine spongiform encephalopathy;
and
(ii) diagnostic tools and preventive and
therapeutic agents for foot and mouth disease,
bovine spongiform encephalopathy, variant
Creutzfeldt-Jacob disease, and related
diseases;
(K) plans for providing appropriate compensation
for affected animals in the event of the introduction
of foot and mouth disease, bovine spongiform
encephalopathy, or related diseases into the United
States; and
(L) recommendations to Congress for legislation
that will improve efforts to assess, prevent, or
control the transmission of foot and mouth disease,
bovine spongiform encephalopathy, variant Creutzfeldt-
Jacob disease, and related diseases in the United
States and in other countries.
(c) Consultation.--
(1) Preliminary report.--In preparing the preliminary
report under subsection (a), the Secretary shall consult with--
(A) the Secretary of the Treasury
(B) the Secretary of Commerce;
(C) the Secretary of State;
(D) the Secretary of Health and Human Services;
(E) the Secretary of Defense;
(F) the United States Trade Representative;
(G) the Director of the Federal Emergency
Management Agency; and
(H) representatives of other appropriate Federal
agencies;
(2) Final report.--In preparing the final report under
subsection (b), the Secretary shall consult with--
(A) the individuals listed in paragraph (1);
(B) private and nonprofit sector experts in
infectious disease, research, prevention, and control;
(C) international, State, and local governmental
animal health officials;
(D) private, nonprofit, and public sector livestock
experts;
(E) representatives of blood collection and
distribution entities; and
(F) representatives of consumer and patient
organizations and other interested members of the
public.
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